Watland Solbjørg, Solberg Nes Lise, Hanson Elizabeth, Ekstedt Mirjam, Stenberg Una, Børøsund Elin
Department of Digital Health Research, Division of Medicine, Oslo University Hospital, Oslo, Norway.
Medicine Intensive Care Unit, Department of Acute Medicine, Division of Medicine, Oslo University Hospital, Oslo, Norway.
JMIR Form Res. 2023 Apr 25;7:e46299. doi: 10.2196/46299.
Family caregivers of patients who are critically ill have a high prevalence of short- and long-term symptoms, such as fatigue, anxiety, depression, symptoms of posttraumatic stress, and complicated grief. These adverse consequences following a loved one's admission to an intensive care unit (ICU) are also known as post-intensive care syndrome-family. Approaches such as family-centered care provide recommendations for improving the care of patients and families, but models for family caregiver follow-up are often lacking.
This study aims to develop a model for structuring and individualizing the follow-up of family caregivers of patients who are critically ill, starting from the patients' ICU admission to after their discharge or death.
The model was developed through a participatory co-design approach using a 2-phased iterative process. First, the preparation phase included a meeting with stakeholders (n=4) for organizational anchoring and planning, a literature search, and interviews with former family caregivers (n=8). In the subsequent development phase, the model was iteratively created through workshops with stakeholders (n=10) and user testing with former family caregivers (n=4) and experienced ICU nurses (n=11).
The interviews revealed how being present with the patient and receiving adequate information and emotional care were highly important for family caregivers at an ICU. The literature search underlined the overwhelming and uncertain situation for the family caregivers and identified recommendations for follow-up. On the basis of these recommendations and findings from the interviews, workshops, and user testing, The Caregiver Pathway model was developed, encompassing 4 steps: within the first few days of the patient's ICU stay, the family caregivers will be offered to complete a digital assessment tool mapping their needs and challenges, followed by a conversation with an ICU nurse; when the patient leaves the ICU, a card containing information and support will be handed out to the family caregivers; shortly after the ICU stay, family caregivers will be offered a discharge conversation by phone, focusing on how they are doing and whether they have any questions or concerns; and within 3 months after the ICU stay, an individual follow-up conversation will be offered. Family caregivers will be invited to talk about memories from the ICU and reflect upon the ICU stay, and they will also be able to talk about their current situation and receive information about relevant support.
This study illustrates how existing evidence and stakeholder input can be combined to create a model for family caregiver follow-up at an ICU. The Caregiver Pathway can help ICU nurses improve family caregiver follow-up and aid in promoting family-centered care, potentially also being transferrable to other types of family caregiver follow-up.
重症患者的家庭照顾者出现短期和长期症状的比例很高,如疲劳、焦虑、抑郁、创伤后应激症状和复杂悲伤。亲人入住重症监护病房(ICU)后的这些不良后果也被称为重症监护后综合征-家庭型。以家庭为中心的护理等方法为改善患者及家庭护理提供了建议,但家庭照顾者随访模式往往缺失。
本研究旨在建立一个模式,从患者入住ICU到出院或死亡后,对重症患者的家庭照顾者进行结构化和个性化随访。
该模式通过参与式协同设计方法,采用两阶段迭代过程开发。首先,准备阶段包括与利益相关者(n = 4)开会进行组织定位和规划、文献检索以及对前家庭照顾者(n = 8)进行访谈。在随后的开发阶段,通过与利益相关者(n = 10)举办研讨会以及对前家庭照顾者(n = 4)和经验丰富的ICU护士(n = 11)进行用户测试,迭代创建该模式。
访谈揭示了在ICU陪伴患者以及获得充分信息和情感关怀对家庭照顾者极为重要。文献检索强调了家庭照顾者面临的压倒性和不确定性情况,并确定了随访建议。基于这些建议以及访谈、研讨会和用户测试的结果,开发了照顾者路径模型,包括4个步骤:在患者入住ICU的头几天内,将为家庭照顾者提供一个数字评估工具,以了解他们的需求和挑战,随后与一名ICU护士进行交谈;当患者离开ICU时,将向家庭照顾者发放一张包含信息和支持内容的卡片;在患者离开ICU后不久,将通过电话与家庭照顾者进行出院交谈,重点了解他们的状况以及是否有任何问题或担忧;在患者离开ICU后3个月内,将提供一次个性化随访交谈。将邀请家庭照顾者谈论在ICU的回忆并反思在ICU的经历,他们还能够谈论自己的当前状况并获得有关相关支持的信息。
本研究说明了如何将现有证据和利益相关者的意见相结合,以创建一个ICU家庭照顾者随访模式。照顾者路径可以帮助ICU护士改善对家庭照顾者的随访,并有助于促进以家庭为中心的护理,可能也适用于其他类型的家庭照顾者随访。